A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984038



Internal ID20551078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75104436..75105308hg38UCSC Ensembl
chr10:76864194..76865066hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445994
Supporting Variants
Samples
Known GenesDUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer